A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502999



Internal ID279847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32842387..32842480hg38UCSC Ensembl
chr13:33416525..33416618hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686736
Samples
Known GenesLINC00423
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502999
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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